MODIFICATION TO AURORA MRI SYSTEM— 510(k) K073425

Substantially Equivalent

Aurora Imaging Technology, Inc.

FDA 510(k) clearance K073425 for MODIFICATION TO AURORA MRI SYSTEM, Substantially Equivalent on 2008-09-16. Applicant: Aurora Imaging Technology, Inc..

Clearance details

Applicant: Aurora Imaging Technology, Inc.
Product code: Code LNH
Advisory panel: Radiology
Date received: 2007-12-03
Decision date: 2008-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Andover, MA, US

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Adverse events under product code LNH

product code LNH

Death: 11
Injury: 670
Malfunction: 1,460
Other: 2
Total: 2,143

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.